BEUDAMED
    29 results · 20ms · Sources: EU EUDAMED, US FDA

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    NIDO Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07315K0112060·Tap, 6.50mm

    CosmoLock Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07311K0112060·Tap, 8.5 mm

    InSePtion MIS Fixation System

    FDA UDI
    Kalitec Direct LLC·B07314K0112060·Punch, 6 and 8 mm

    PARALLAX BONE AND VERTEBRAL BODY BIOPSY AND INFUSION NEEDLES

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    ROLLO 112X120X12E/PRINTER

    FDA UDI
    AB MEDICA GROUP, S.A.·08428763004806·

    CoverLoc™ Volar Plate

    FDA UDI
    TORNIER, INC.·00846832001125·VOLAR PLATE

    FLEXIBLE TIP THERMOMETER, MODEL 011206

    FDA 510(k)
    FDA Class 2 ·General Hospital

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707101307·BMX-MINI PALATAL EXP. DIRECT 6MMX12MM .

    DIMENSION ENZYMATIC CARBONATE (ECO2) FLEX METHOD, CATALOG DF137

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    AMYSEAT TILT/RECLINE SEATING

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    PYRAMESH C TITANIUM MESH

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDIC, INC.·Product code EZX·August 12, 2011

    PYRAMESH

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code EZX·September 29, 2015

    CA090, DIRECT DRIVE LCA 3/BX

    FDA Adverse Event
    Malfunction ·APPLIED MEDICAL RESOURCES·Product code FZP·October 11, 2016

    AKREOS ADVANCED OPTICS ASPHERIC LENS

    FDA Adverse Event
    Injury ·BAUSCH & LOMB·Product code HQL·October 21, 2011

    ASTERX EXPANDABLE CORPECTOMY SYSTEM

    FDA Adverse Event
    Injury ·MSD DEGGENDORF MFG·Product code MQP·March 4, 2019

    ASTERX EXPANDABLE CORPECTOMY SYSTEM

    FDA Adverse Event
    Injury ·MSD DEGGENDORF MFG·Product code MQP·March 4, 2019

    PYRAMESH C TITANIUM MESH

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code EZX·October 26, 2019

    FREESTYLE

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC., USA·Product code LFR·May 11, 2007

    TOTALCARE BED

    FDA Adverse Event
    Other ·HILL-ROM, INC.·Product code FNL·March 15, 2013

    AUTOPULSE® RESUSCITATION SYSTEM MODEL 100

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION, INC·Product code DRM·August 14, 2014